Relevant bibliographies by topics / Access to health care

Academic literature on the topic 'Access to health care'

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Published: 4 June 2021
Last updated: 26 January 2023

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Journal articles on the topic "Access to health care"

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Wright, L. D. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00026.

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Storniolo, Cosimo N. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00027.

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Greenberg, Henry. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00028.

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West, Burton C. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00029.

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Esham, Richard H. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00030.

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Berman, Julian L. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00031.

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Amerling, Richard. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00032.

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Maddrey, Willis C. "Access to Health Care." Annals of Internal Medicine 118, no. 3 (February 1, 1993): 232. http://dx.doi.org/10.7326/0003-4819-118-3-199302010-00033.

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Sommaripa, Amory M. "Access to Health Care." Annals of Internal Medicine 113, no. 2 (July 15, 1990): 168. http://dx.doi.org/10.7326/0003-4819-113-2-168.

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Gourevitch, Marc. "Access to Health Care." Annals of Internal Medicine 113, no. 6 (September 15, 1990): 478. http://dx.doi.org/10.7326/0003-4819-113-6-478.

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Dissertations / Theses on the topic "Access to health care"

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Blanton, Sandra. "Justice in Health Care Access Measuring Attitudes of Health Care Professionals." TopSCHOLAR®, 2000. http://digitalcommons.wku.edu/theses/714.

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To measure attitudes toward justice in access to health care services in managed care plans in a convenience sample of medical professionals at Clark Memorial Hospital in Jeffersonville, Indiana. Methods. A sixteen item, self-administered instrument based on Morreim's four concepts of justice in health care access was administered to 147 health care professionals, representing physicians, allied health, and hospital administration. SPSS was used to analyze the results. Results. The attitudes of the respondents were negative toward managed care. They did not feel that managed care had been a positive development in the United States or that managed care had improved access to preventive care or improved primary care. On the survey instrument, respondents scored highest on the scale measuring fairness to individual patients. Conclusion. In a convenience sample of health care professionals at Clark Memorial Hospital in Jeffersonville, Indiana, equity in distributing access to health care among individual patient needs was found to more closely meet their expectations of justice in health care access. There were no differences found across occupational groups in their responses to the two scales. There were differences in attitudes toward managed care among occupational groups.
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Fike, Verinda Jean Esther. "Health insurance and health care access in China." CONNECT TO ELECTRONIC THESIS, 2008. http://dspace.wrlc.org/handle/1961/5527.

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Marshall, Emily Gard. "Universal health care? : access to primary care and missed health care of young adult Canadians." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/30948.

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Prevalence of missed health care by life course stage is examined with a critique of the measure of missed care. Canadians reporting missed care has increased from 4.2% in 1995 to 12.5% in 2001. Research questions: 1. Who reports missed care in Canada? 2. What are the relationships among life course stages, social support, predisposing, enabling and need factors to the reporting of missed care? 3. What is the role that life course stages play in the relationships among social support, predisposing, enabling, and need factors? 4. What kinds of health care are Canadians reporting they missed? 5. What reasons are provide for missing care?; and 6. Who accesses primary care and what is the relationship to reporting missed care? Methods: Analysis was done using the Canadian Community Health Survey Cycle 2.1. Nested multiple logistic regression models explore the relationships among variables of interest predicting missed care. Results: Young adults (18-30) are more likely to report missed care compared to other age groups and are least likely to have a regular doctor. Social support is most significantly protective against missed care for young adults. Weak sense of belonging to a local community and lower income are stronger predictors of missed care for young adults. Young adults differ from others in the reasons they report for missed care (i.e., more likely to report cost as a barrier). Discussion: It's not clear if the difference between young adults and other life course stages is in actual missed care or expectations of primary care. Yet, the literature on emerging adulthood invites curiosity about how delayed adulthood leaves them in less stable, financially insecure, socially and institutionally isolated situations that have subsequent consequences for primary care access. Changes in models of primary care have led to a decline in comprehensive care and more drop-in clinics; while, not having a regular doctor is associated with missed care. If patterns of inadequate primary care access established in young adulthood are perpetuated in later life, this may foretell undesirable consequences for the health of Canadians. A new model for measuring unmet health care needs is proposed.
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Smith, Raymond Joshua. "Frontier residents' perceptions of health care access." Thesis, Montana State University, 2008. http://etd.lib.montana.edu/etd/2008/smith/SmithR0508.pdf.

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It can be difficult to access health care due to cost, lack of insurance, and lack of available resources for Americans today. Frontier persons have even more obstacles in accessing health care due to geography, time and distance to facilities, lack of medical personal, and culture. This study's purpose was to better understand frontier residents' perceptions of access to health care. Specific aims were to (a) explore frontier residents' health care access resources, (b) investigate frontier residents' utilization of health care services, (c) search for reasons frontier residents seek health care (d) and explore the residents' overall satisfaction regarding their health care access options. A qualitative approach that included open-ended questions was used to interview a convenience sample of 11 frontier residents in a Southwestern Montana town. Participants were recruited using a snowball approach. Common themes were extracted using a "low inference" analysis style. Aday and Andersen's framework and their study of access to medical care (1975) guided the study. Results revealed most residents felt they had access to health care and all had seen a provider in the last 2 years. Residents used "local" services, the closest being 70 miles away, for minor ailments and injuries or when home remedies failed. A "by-pass" mentality of "local" services was seen for more serious events. Children were treated differently and health care was sought sooner if they became ill. Reasons for seeking care included preventative services, acute injuries, and infectious processes. Cost, weather, road conditions, gas prices, travel time, and taking time off work were mentioned as barriers in health care utilization. Insurance deductibles and costs of health services limited the type of health care residents sought. Satisfactions with health care providers were high as well as sliding scale fees of the local health centers. Cost and distance were unsatisfactory. Implications for practice include educating residents about benefits and abilities of their local resources, the need to seek care for preventative services, health promotion topics, and disease prevention. In addition, health care authorities should focus on alternative ways to bring health care to the frontier residents including telemedicine and lowering costs.
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Kama, Zukiswa Shirley. "An evaluation of access to health care : Gugulethu Community Health Clinic." Thesis, Cape Peninsula University of Technology, 2017. http://hdl.handle.net/20.500.11838/2456.

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Thesis (MTech (Public Management))--Cape Peninsula University of Technology, 2017.
The purpose of this study was to examine the problem of access to health care centres in the Western Cape and to forward recommendations that will improve access to health care facilities in the Western Cape. The first objective of the study was to identify trends in primary health care looking at Nigeria, with the view of learning lessons of experience. Secondly, the study provided an overview of the South African health care system. The study further examined the problems around access to Gugulethu Community Health Clinic. The research objectives were directly linked to the composition of chapters. The study utilised a mixed-method approach of quantitative and qualitative approaches. This method is called multi-method approach. The purpose of combining the two approaches was to understand the research problem from a subjective and objective point of view, as well as to provide an in-depth understanding of a research topic, which led to more reliable research results. Data collection was acquired by utilising a structured questionnaire and personal observations. Two groups of respondents participated in the study inter alia: the patients and the staff of Gugulethu Community Health Clinic.
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Vedom, Julia. "Health care access and regional disparities in China." Thesis, University of Ottawa (Canada), 2008. http://hdl.handle.net/10393/25483.

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This thesis examines the access of health care facilities in nine provinces of China between the years 1989 and 2004, evaluating the effect of demographic, financial and geographic factors. Equity in social welfare has long played a major role in shaping China's national policies. However, continued pursuit of the GDP-led development orientation in China since the late 1970s has resulted in increasing urban-rural and intra- and inter-regional socio-economic disparities, raising multiple causes for concern from an equity perspective and suggesting the trends that should be closely monitored. While there is a consensus about the need and importance of access equity, little geographic research has been conducted in this area. In light of these issues, using China Health and Nutrition Survey this study addressed the following two objectives: (1) to describe the geographic and financial disparities in access to clinics and hospitals in nine provinces of China during the 1989-2004 period, and (2) to explore the demographic, socio-economic and geographic factors affecting access to health care. Results of the analysis show that between 1989 and 2004 the accessibility gap between hospitals and clinics in terms of geographic indicators has decreased, while the gap in financial accessibility has increased, making urban hospitals the least accessible facilities. Access to both hospitals and clinics in urban and rural areas is mostly conditioned by geographic factors, namely the travel method, region of residence and the availability of health care facilities. Patients who were able to reach the facilities on foot were more likely to enjoy better access than those who were not able to do so. Similarly, residents of western China (Guangxi and Guizhou) along with the provinces with higher availability of health care facilities also tended to have better potential access than their counterparts. Several important contributions essential for informing public decision- and policymaking stem from this thesis, leading to a better understanding of issues related to the accessibility of health care in nine provinces of China. While, typically, the determinants of accessibility have been attributed to the financial or demographic characteristics of patients, this research has identified geographic factors as being of the foremost importance in the accessibility of health care. This important finding provides grounds for further geographic research on accessibility issues in China. While our conceptual framework was designed for studying the accessibility of health care in China, it can be potentially applied to any country with regional, provincial or neighborhood disparities in access.
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Morrisey, Karyn Marie. "Access to health care services in rural ireland." Thesis, University of Leeds, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.502767.

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Castro, Beatriz. "Access control regulation in the health care sector." Thesis, Stockholms universitet, Juridiska institutionen, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-156879.

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This thesis is about access control in the health care sector. Access control is a function in It-systems that allows authorized users to access data they have right to access, prevents unauthorized users from accessing data and prevents authorized users from disclosing data unlawfully. One of the pillars of access control is that a user only is authorized to access data that he or she needs to perform a task. This describes the principle of least privilege and its objective is to ensure data's confidentiality and integrity. In the health care sector where an increasing number of public and private actors are processing sensitive data the application of this principle is essential to protect patients' privacy and confidence in the system. The lawmaker has incorporated the principle of least privilege in legal bodies such as the General Data Protection Regulation, Patient Data Act and the regulation of registers that allow processing of health data. This thesis examines how the lawmaker has incorporated the principle of least privilege to protect health data. Therefore, it examines access control regulation, in particular, requirements on management of access rights and log audits. The lawmaker has applied this principle through requirements on the system that should be incorporated by default and through requirements on management of access rights. The conclusion is that given that the tendency in health care, like in other sectors, is toward automation and more focus on self-care, the requirements should be directed more to systems than medical staff.
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Abbasgholizadeh, Rahimi Samira. "Prioritization of patients' access to health care services." Doctoral thesis, Université Laval, 2017. http://hdl.handle.net/20.500.11794/27499.

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L'accès aux services de santé et les longs délais d'attente sont l’un des principaux problèmes dans la plupart des pays du monde, dont le Canada et les États-Unis. Les organismes de soins de santé ne peuvent pas augmenter leurs ressources limitées, ni traiter tous les patients simultanément. C'est pourquoi une attention particulière doit être portée à la priorisation d'accès des patients aux services, afin d’optimiser l’utilisation de ces ressources limitées et d’assurer la sécurité des patients. En fait, la priorisation des patients est une pratique essentielle, mais oubliée dans les systèmes de soins de santé à l'échelle internationale. Les principales problématiques que l’on retrouve dans la priorisation des patients sont: la prise en considération de plusieurs critères conflictuels, les données incomplètes et imprécises, les risques associés qui peuvent menacer la vie des patients durant leur mise sur les listes d'attente, les incertitudes présentes dans les décisions des cliniciens et patients, impliquant l'opinion des groupes de décideurs, et le comportement dynamique du système. La priorisation inappropriée des patients en attente de traitement a une incidence directe sur l’inefficacité des prestations de soins de santé, la qualité des soins, et surtout sur la sécurité des patients et leur satisfaction. Inspirés par ces faits, dans cette thèse, nous proposons de nouveaux cadres hybrides pour prioriser les patients en abordant un certain nombre de principales lacunes aux méthodes proposées et utilisées dans la littérature et dans la pratique. Plus précisément, nous considérons tout d'abord la prise de décision collective incluant les multiples critères de priorité, le degré d'importance de chacun de ces critères et de leurs interdépendances dans la procédure d'établissement des priorités pour la priorisation des patients. Puis, nous travaillons sur l'implication des risques associés et des incertitudes présentes dans la procédure de priorisation, dans le but d'améliorer la sécurité des patients. Enfin, nous présentons un cadre global en se concentrant sur tous les aspects mentionnés précédemment, ainsi que l'implication des patients dans la priorisation, et la considération des aspects dynamiques du système dans la priorisation. À travers l'application du cadre global proposé dans le service de chirurgie orthopédique à l'hôpital universitaire de Shohada, et dans un programme clinique de communication augmentative et alternative appelé PACEC à l'Institut de réadaptation en déficience physique de Québec (IRDPQ), nous montrons l'efficacité de nos approches en les comparant avec celles actuellement utilisées. Les résultats prouvent que ce cadre peut être adopté facilement et efficacement dans différents organismes de santé. Notamment, les cliniciens qui ont participé à l'étude ont conclu que le cadre produit une priorisation précise et fiable qui est plus efficace que la méthode de priorisation actuellement utilisée. En résumé, les résultats de cette thèse pourraient être bénéfiques pour les professionnels de la santé afin de les aider à: i) évaluer la priorité des patients plus facilement et précisément, ii) déterminer les politiques et les lignes directrices pour la priorisation et planification des patients, iii) gérer les listes d'attente plus adéquatement, vi) diminuer le temps nécessaire pour la priorisation des patients, v) accroître l'équité et la justice entre les patients, vi) diminuer les risques associés à l’attente sur les listes pour les patients, vii) envisager l'opinion de groupe de décideurs dans la procédure de priorisation pour éviter les biais possibles dans la prise de décision, viii) impliquer les patients et leurs familles dans la procédure de priorisation, ix) gérer les incertitudes présentes dans la procédure de prise de décision, et finalement x) améliorer la qualité des soins.
Access to health care services and long waiting times are one of the main issues in most of the countries including Canada and the United States. Health care organizations cannot increase their limited resources nor treat all patients simultaneously. Then, patients’ access to these services should be prioritized in a way that best uses the scarce resources, and to ensure patients’ safety. In fact, patients’ prioritization is an essential but forgotten practice in health care systems internationally. Some challenging aspects in patients’ prioritization problem are: considering multiple conflicting criteria, incomplete and imprecise data, associated risks that threaten patients on waiting lists, uncertainties in clinicians’ decisions, involving a group of decision makers’ opinions, and health system’s dynamic behavior. Inappropriate prioritization of patients waiting for treatment, affects directly on inefficiencies in health care delivery, quality of care, and most importantly on patients’ safety and their satisfaction. Inspired by these facts, in this thesis, we propose novel hybrid frameworks to prioritize patients by addressing a number of main shortcomings of current prioritization methods in the literature and in practice. Specifically, we first consider group decision-making, multiple prioritization criteria, these criteria’s importance weights and their interdependencies in the patients’ prioritization procedure. Then, we work on involving associated risks that threaten patients on waiting lists and handling existing uncertainties in the prioritization procedure with the aim of improving patients’ safety. Finally, we introduce a comprehensive framework focusing on all previously mentioned aspects plus involving patients in the prioritization, and considering dynamic aspects of the system in the patients’ prioritization. Through the application of the proposed comprehensive framework in the orthopedic surgery ward at Shohada University Hospital, and in an augmentative and alternative communication (AAC) clinical program called PACEC at the Institute for Disability Rehabilitation in Physics of Québec (IRDPQ), we show the effectiveness of our approaches comparing the currently used ones. The implementation results prove that this framework could be adopted easily and effectively in different health care organizations. Notably, clinicians that participated in the study concluded that the framework produces a precise and reliable prioritization that is more effective than the currently in use prioritization methods. In brief, the results of this thesis could be beneficial for health care professionals to: i) evaluate patients’ priority more accurately and easily, ii) determine policies and guidelines for patients’ prioritization and scheduling, iii) manage waiting lists properly, vi) decrease the time required for patients’ prioritization, v) increase equity and justice among patients, vi) diminish risks that could threaten patients during waiting time, vii) consider all of the decision makers’ opinions in the prioritization procedure to prevent possible biases in the decision-making procedure, viii) involve patients and their families in the prioritization procedure, ix) handle available uncertainties in the decision-making procedure, and x) increase quality of care.
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Norton, Lavinia Jane. "Individual responsibility, justice and access to health care." Thesis, University of Leeds, 2001. http://etheses.whiterose.ac.uk/977/.

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The aim of this thesis is to examine whether it is morally defensible to use lifestyle as one of the criteria for rationing health care. I argue that it is not justifiable to use former lifestyle to select patients for treatment. Chapter one outlines the principles of the NHS and discusses the reality of rationing in health care provision in Britain. I maintain that there is a prima facie legal and moral right to health care and explore whether this right imposes a responsibility on individuals to maintain a healthy lifestyle. Chapter two critically examines some of the criteria, which are used to ration health care. Government policy documents, such as 'The New NHS: Modern.Dependable.' (Department of Health 1997: 13) suggest that patients should be treated 'according to need and need alone.' I argue that the concept of medical need is indeed one of the proper criteria for the distribution of medical resources. However, it is not the only relevant criterion and should be considered along with other factors such as patient choice, clinical and cost effectiveness. Other criteria including age and lifestyle may also be relevant, but in so far as they affect the probable clinical outcomes of treatment. Chapter three clarifies some of the contemporary approaches to distributive justice and explores their implications for the allocation of health care between individuals. I suggest that an eclectic approach should be adopted where consideration is given both to promoting individual choices about lifestyles and protecting the welfare of the community. None of these theories of justice suggest that taking lifestyle into account when allocating scarce resources must be unjust. Chapter four investigates whether individuals should be held responsible for their lifestyle. I argue that some health related behaviour is voluntary and therefore people might be held responsible for the consequences of their behaviour. However, in many cases health related behaviour may not be voluntary, because it may have been unduly influenced by factors beyond the control of the individual. Even if it is voluntary, it may be justifiable or excusable in some cases. I discuss whether risk takers deserve any blame, and maintain that withdrawal or delay of medical treatment as a punishment for former lifestyle is always wrong. Chapter five argues that it is essential for health care professionals to inform people of risks to their health. This does not interfere with their liberty, and allows them to make choices based upon their own values. I also examine whether it is justifiable to use more coercive strategies, such as persuasion, manipulation and legal prohibition in order to encourage people to maintain a healthy lifestyle. Chapter six argues that it is not possible to implement a policy to ration health care partly on the basis of lifestyle in a fair way. I propose an alternative policy, which involves taxation on certain products associated with risk. Chapter seven examines a variety of cases of rationing based on lifestyle. I conclude that rationing according to former lifestyle is not morally defensible.
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Books on the topic "Access to health care"

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Beauregard, Karen. Access to health care. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1991.

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Donatelle, Rebecca J. Access to health. 8th ed. San Francisco: Benjamin Cummings, 2004.

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Access to health. San Francisco: Benjamin Cummings, 2010.

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Access to health. 7th ed. San Francisco: Benjamin Cummings, 2002.

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Access to health. San Francisco: Pearson Benjamin Cummings, 2008.

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Access to health. 9th ed. San Francisco: Pearson/Benjamin Cummings, 2006.

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Health, Washington (State) Dept of Health Community and Family. Children's access to health care report. [Olympia? Wash.]: The Dept., 1994.

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Goddard, Maria. Equity of access to health care. York: Centre for Health Economics, University of York, 1998.

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Authority, Montana Health Care. Statewide universal health care access plans. Helena: Montana Health Care Authority, 1994.

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L, Millman Michael, ed. Access to health care in America. Washington, D.C: National Academy Press, 1993.

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Book chapters on the topic "Access to health care"

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Orbell, Sheina, Havah Schneider, Sabrina Esbitt, Jeffrey S. Gonzalez, Jeffrey S. Gonzalez, Erica Shreck, Abigail Batchelder, et al. "Health Care Access." In Encyclopedia of Behavioral Medicine, 908. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1005-9_882.

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Allebeck, Peter. "Health Care Access." In Encyclopedia of Behavioral Medicine, 1000. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-39903-0_882.

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Begley, Charles Edward. "Access to Care." In Encyclopedia of Immigrant Health, 145–49. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-5659-0_10.

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Baggott, Rob. "Access to Health Care." In Health and Health Care in Britain, 188–212. London: Macmillan Education UK, 2004. http://dx.doi.org/10.1007/978-1-137-11638-3_8.

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Riedel, Ruth Lyn. "Access to Health Care." In Handbook of Immigrant Health, 101–23. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-1936-6_6.

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Quill, Beth E. "Access to Health Care." In Encyclopedia of Women’s Health, 22–24. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48113-0_8.

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Forbis, Shalini G. "Child Health Care Access." In Encyclopedia of Immigrant Health, 410–12. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-5659-0_133.

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Notaro, Sheri R. "Access to Health Care." In Marginality and Global LGBT Communities, 53–74. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-22415-8_3.

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O’Shea, Daniel J. "Access to Care." In Mental Health Practitioner's Guide to HIV/AIDS, 69–74. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5283-6_4.

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Daniel, Susan J., and Sajeesh Kumar. "Access to Oral Care Through Teledentistry." In Health Informatics, 65–74. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-08973-7_7.

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Conference papers on the topic "Access to health care"

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Miller, G., J. Dorsey, and G. Hermes. "54. Access Control Options for High Power Lasers." In AIHce 1996 - Health Care Industries Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765165.

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Mirkovic, Jelena, Haakon Bryhni, and Cornelia M. Ruland. "Secure solution for mobile access to patient's health care record." In 2011 IEEE 13th International Conference on e-Health Networking, Applications and Services (Healthcom 2011). IEEE, 2011. http://dx.doi.org/10.1109/health.2011.6026769.

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Tanenhaus, Robert. "Economics of health care access and delivery projects." In Health Care Technology Policy II: The Role of Technology in the Cost of Health Care: Providing the Solutions, edited by Warren S. Grundfest. SPIE, 1995. http://dx.doi.org/10.1117/12.225313.

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Ariyani, Devi Eka, Kristina Setyowati, and Rutiana D. Wahyunengseh. "Inclusive Health Care Access of Shackling-Free Program." In Proceedings of the Annual Civic Education Conference (ACEC 2018). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/acec-18.2018.51.

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Chowdhury Bonhi, Tasmeem. "ACCESS TO EYE HEALTH CARE: BARRIERS WOMEN FACE IN BANGLADESH." In Global Public Health Conference. The International Institute of Knowledge Management, 2019. http://dx.doi.org/10.17501/26138417.2019.2201.

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Shanmugam, Murugaraj, Srinath Thiruvengadam, Assadarat Khurat, and Ilias Maglogiannis. "Enabling Secure Mobile Access for Electronic Health Care Applications." In 2006 Pervasive Health Conference and Workshops. IEEE, 2006. http://dx.doi.org/10.1109/pcthealth.2006.361689.

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Yasnoff, William A., Edward L. Tomkins, and Louise M. Dunn. "Physician access to drug profiles to reduce adverse reactions." In Health Care Technology Policy II: The Role of Technology in the Cost of Health Care: Providing the Solutions, edited by Warren S. Grundfest. SPIE, 1995. http://dx.doi.org/10.1117/12.225311.

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Bahçe, Serdal, Altuğ Murat Köktas, and Deniz Abukan. "Health Care Reform and Household Welfare: Health Transformation Programme in Turkey." In International Conference on Eurasian Economies. Eurasian Economists Association, 2013. http://dx.doi.org/10.36880/c04.00718.

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We assessed the health care reform and its effects on household’s welfare such as access to health care and household economic burden. We used descriptive analysis on 2002-2011 Ministry of Health and OECD Health Statistics. The main result is about using health care. Access to health care increased after health care reform in Turkey. Number of applications to health care service server and its units rose. On the other hand, financial burden of health care on household’s budget decreased number of applications. The main result percentage of not consulting a specialist even needed to consult a specialist but did not during the past 12 months is %4.9 in 2003 and %19.9 in 2010. To improve health care access, policy makers should improve public sector provision of health care, increase social security benefit packages and protect poor and vulnerable.
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Cartmell, John. "Predictive Inter-Radio Access Technology Handover." In Imaging and Signal Processing in Health Care and Technology. Calgary,AB,Canada: ACTAPRESS, 2012. http://dx.doi.org/10.2316/p.2012.773-020.

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Jie Song, Binfeng Li, Yao Yang, Su Wu, and Paul Griffin. "Improving Health Care access by optimizing the allocation network of community health centers." In 2008 IEEE International Conference on Service Operations and Logistics, and Informatics (SOLI). IEEE, 2008. http://dx.doi.org/10.1109/soli.2008.4686532.

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Reports on the topic "Access to health care"

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Williams, Kristine. Improving Transportation Access to Health Care Services. Tampa, FL: University of South Florida, February 2018. http://dx.doi.org/10.5038/cutr-nctr-rr-2018-09.

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Jaffee, Eleanor, Joan Widmer, and Lisa Speropolous. Oral Health Care Access in New Hampshire. University of New Hampshire Libraries, 2015. http://dx.doi.org/10.34051/p/2020.234.

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Courtemanche, Charles, James Marton, Benjamin Ukert, Aaron Yelowitz, and Daniela Zapata. Early Effects of the Affordable Care Act on Health Care Access, Risky Health Behaviors, and Self-Assessed Health. Cambridge, MA: National Bureau of Economic Research, March 2017. http://dx.doi.org/10.3386/w23269.

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Damiano, Peter C., Elizabeth T. Momany, Norman S. J. Foster, and Hermine E. McLeran. Transportation of Rural Elders and Access to Health Care. Iowa City, Iowa: University of Iowa Public Policy Center, February 1995. http://dx.doi.org/10.17077/fska-7sh3.

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Keenan, Teresa A. Health Care in Rural America: Use, Affordability, and Access. Washington, DC: AARP Research, November 2021. http://dx.doi.org/10.26419/res.00447.001.

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Rashida, Gul, Iram Kamran, Muhammad Khalil, Zeba Tasneem, Rehan Niazi, Mumraiz Khan, and Tahira Parveen. Increasing access to reproductive health care through improved service delivery. Population Council, 2017. http://dx.doi.org/10.31899/rh7.1027.

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Gresenz, Carole Roan, Jeannette Rogowski, and José Escarce. Social Networks and Access to Health Care Among Mexican-Americans. Cambridge, MA: National Bureau of Economic Research, October 2007. http://dx.doi.org/10.3386/w13460.

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McKernan, Susan C., Julie C. Reynolds, Astha Singhal, Raymond Kuthy, and Peter C. Damiano. Access to Dental Care and the Oral Health Safety Net. Iowa City, Iowa: University of Iowa Public Policy Center, September 2013. http://dx.doi.org/10.17077/0ar2-nfu2.

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Chatterji, Pinka, Sandra Decker, and Jason Huh. Medicaid Physician Fees and Access to Care among Children with Special Health Care Needs. Cambridge, MA: National Bureau of Economic Research, February 2020. http://dx.doi.org/10.3386/w26769.

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Werbeck, Anna, Ansgar Wübker, and Nicolas Ziebarth. Cream Skimming by Health Care Providers and Inequality in Health Care Access: Evidence from a Randomized Field Experiment. Cambridge, MA: National Bureau of Economic Research, May 2021. http://dx.doi.org/10.3386/w28809.

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